Biomedical Scientist

Proclinical is currently recruiting for a Biomedical Scientist for a medical technology and devices company located in Mount Laurel, NJ.

Job Responsibilities:

• Participate as a team member in an entrepreneurial environment with the goal of developing new device treatments in the area of heart failure.
• Responsible for designing preclinical studies and writing protocols.
• Responsible for defining, planning, and monitoring preclinical study project parameters (protocol, timeline, budget, and pricing) and to establish a study implementation strategy that meets strict GLP requirements.
• Responsible for the creation of study plan and the tracking of milestones for assigned projects on a proactive basis.
• Generate, analyze, and review data.
• Act as the Company's representative and Study Sponsor for studies.
• Maintain close communications with internal and external contacts to ensure that studies remain on schedule, within budget, and appropriately resourced.
• Responsible for developing, executing, and managing pre-clinical (animal) study protocols under strict GLP rules.

Skills and Requirements:

• At a minimum Bachelor's degree in the biomedical sciences (e.g. medical technology, biology, animal science, biomedical science, nursing) or engineering (e.g. biomedical engineering) required.
• Advanced degrees (e.g. M.Sc., Ph.D., DVM) preferable.
• At least 4 years of experience developing, executing, and managing study protocols under GLP.
• Thorough understanding of standards and practices that regulate preclinical safety and effectiveness studies.
• Proven experience in the development, planning, execution, and reporting of preclinical safety and effectiveness studies for medical devices.
• Proactive in their approach to the job and have the ability to work in a "start-up" environment and function well in identifying priorities without constant supervision.
• Have the flexibility to work on multiple projects and changing priorities while complying with plans and schedules for projects in his/her area of responsibility.
• Significant practical experience and theoretical knowledge of Design of Experiments, data collection, data processing, and statistics for preclinical studies required.
• Experience with biocompatibility assurance required.
• Excellent animal laboratory practical skills.
• Work experience in the Medical Devices Industry or CRO required.
• Experience with cardiovascular devices highly desirable.
• Experience with implantable devices highly desirable.
• Academic publication record highly desirable.
  Responsibilities

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Ysabel Capitan at or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#LI-YC1

#Scientific